Package 67877-775-89

Brand: famotidine

Generic: famotidine
NDC Package

Package Facts

Identity

Package NDC 67877-775-89
Digits Only 6787777589
Product NDC 67877-775
Description

50 mL in 1 BOTTLE (67877-775-89)

Marketing

Marketing Status
Marketed Since 2023-08-24
Brand famotidine
Generic famotidine
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "87b513db-989d-4c31-b597-1af0093d0085", "openfda": {"nui": ["N0000000151", "N0000175784"], "unii": ["5QZO15J2Z8"], "rxcui": ["310274"], "spl_set_id": ["b2228be0-472b-4e47-9910-af0bf12fde77"], "pharm_class_epc": ["Histamine-2 Receptor Antagonist [EPC]"], "pharm_class_moa": ["Histamine H2 Receptor Antagonists [MoA]"], "manufacturer_name": ["Ascend Laboratories, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "50 mL in 1 BOTTLE (67877-775-89)", "package_ndc": "67877-775-89", "marketing_start_date": "20230824"}], "brand_name": "Famotidine", "product_id": "67877-775_87b513db-989d-4c31-b597-1af0093d0085", "dosage_form": "POWDER, FOR SUSPENSION", "pharm_class": ["Histamine H2 Receptor Antagonists [MoA]", "Histamine-2 Receptor Antagonist [EPC]"], "product_ndc": "67877-775", "generic_name": "Famotidine", "labeler_name": "Ascend Laboratories, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Famotidine", "active_ingredients": [{"name": "FAMOTIDINE", "strength": "40 mg/5mL"}], "application_number": "ANDA216400", "marketing_category": "ANDA", "marketing_start_date": "20230824", "listing_expiration_date": "20261231"}